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dc.contributor.authorChow, Brian Y.
dc.contributor.authorHan, Xue
dc.contributor.authorBoyden, Edward Stuart
dc.date.accessioned2016-07-07T16:38:03Z
dc.date.available2016-07-07T16:38:03Z
dc.date.issued2012-02
dc.identifier.isbn9780444594266
dc.identifier.issn00796123
dc.identifier.urihttp://hdl.handle.net/1721.1/103536
dc.description.abstractThe ability to silence, in a temporally precise fashion, the electrical activity of specific neurons embedded within intact brain tissue, is important for understanding the role that those neurons play in behaviors, brain disorders, and neural computations. “Optogenetic” silencers, genetically encoded molecules that, when expressed in targeted cells within neural networks, enable their electrical activity to be quieted in response to pulses of light, are enabling these kinds of causal circuit analyses studies. Two major classes of optogenetic silencer are in broad use in species ranging from worm to monkey: light-driven inward chloride pumps, or halorhodopsins, and light-driven outward proton pumps, such as archaerhodopsins and fungal light-driven proton pumps. Both classes of molecule, when expressed in neurons via viral or other transgenic means, enable the targeted neurons to be hyperpolarized by light. We here review the current status of these sets of molecules, and discuss how they are being discovered and engineered. We also discuss their expression properties, ionic properties, spectral characteristics, and kinetics. Such tools may not only find many uses in the quieting of electrical activity for basic science studies but may also, in the future, find clinical uses for their ability to safely and transiently shut down cellular electrical activity in a precise fashion.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH Director’s Pioneer Award DP2OD002002)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant 1R01NS075421)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant 1R01DA029639)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant 1RC1MH088182)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant 1RC2DE020919)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant 1R01NS067199)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant 1R43NS070453)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (NSF Grant EFRI 0835878)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (NSF Grant DMS 0848804)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (NSF Grant DMS 1042134)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/b978-0-444-59426-6.00003-3en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleGenetically encoded molecular tools for light-driven silencing of targeted neurons [Chapter 3]en_US
dc.typeArticleen_US
dc.identifier.citationChow, Brian Y., Xue Han, and Edward S. Boyden. “Genetically Encoded Molecular Tools for Light-Driven Silencing of Targeted Neurons.” Optogenetics: Tools for Controlling and Monitoring Neuronal Activity (2012): 49–61. (Progress in Brain Research, Vol. 196).en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Media Laboratoryen_US
dc.contributor.mitauthorBoyden, Edward Stuarten_US
dc.relation.journalOptogenetics: Tools for Controlling and Monitoring Neuronal Activityen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsChow, Brian Y.; Han, Xue; Boyden, Edward S.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-0419-3351
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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